Bronchiectasis in teachers & health care workers
I know someone may have the answer to this question. Is there any research on the prevalence of Bronchiectasis diagnosis in current or former teachers and health care workers? Lots of anecdotal information I bet, but is there data to support it?
If the percentage is significant, could this not be a factor that is considered earlier on in the diagnostic process when people have chronic cough, mucus and other symptoms? I’ve read that more people with Bronchiectasis are 60+ women (and predominantly slim build men) , and those with chronic sinusitis issues, low BMI, pectus excavatum, and mitral valve prolapse and ?
With Bronchiectasis becoming more common or properly diagnosed with better imaging, would Medical teaching facilities create a checklist of possible risk factors for a diagnosis of Bronchiectasis? It’s still a rare chronic lung disease of course relative to COPD and asthma. Just wondering about any possible research data and how that trickles down to family doctors. Thanks.
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
This doesn’t answer this question specifically, but I think it’s worth mentioning that there’s a Bronchiectasis and NTM Research Registry. Patients at 24 clinical sites ask their patients if they are are interested in being in the registry and clinical data is collected yearly and available to researchers. My physician at Penn asked me and I enrolled. Here’s info.
https://www.bronchiectasisandntminitiative.org/Research/Registry/Bronchiectasis-and-NTM-Research-Registry
There’s also a patient centered one for those who aren’t near a clinical site.
Sue, I am alittle slow on the reply, but genuinely appreciate your time, guidance and encouragement! 🙂